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  • Hanqian L. Carlson, Satoru Ota, Christine E. Campbell, Peter J. Hurlin
  • Medicine, Biology
  • Human molecular genetics
  • 2001 (First Publication: 1 October 2001)
  • Mutations in Tbx3 are responsible for ulnar-mammary syndrome (UMS), an autosomal dominant disorder affecting limb, tooth, hair, apocrine gland and genital development. Tbx3 is a member of a family ofExpand
  • Satoru Ota, Kuniaki Tsuchiya, Haruhiko Akiyama
  • Biology, Medicine
  • Neuropathology : official journal of the Japanese…
  • 2005 (First Publication: 1 December 2005)
  • We clinicopathologically investigated five autopsy cases of ALS without dementia and with ubiquitinated intraneuronal inclusions. The age at onset of symptoms ranged from 52 to 81 years and theExpand
  • Masatake Kawada, Masao Suzuki, R. Ikeda, Satoru Ota
  • Engineering
  • International Conference on Advances in…
  • 2014 (First Publication: 1 August 2014)
  • Propulsion coils are used for propelling vehicles in superconducting magnetic levitation (Maglev) systems. This paper presents experimental results for finding a propulsion coil with defects by usingExpand
  • Satoru Ota, Kuniaki Tsuchiya, Midori Anno, Kazuhiro Niizato, Haruhiko Akiyama
  • Biology, Medicine
  • Neuropathology : official journal of the Japanese…
  • 2008 (First Publication: 1 February 2008)
  • Late cortical cerebellar atrophy (LCCA) is a neurodegenerative disease which presents with slowly progressive cerebellar ataxia as a prominent symptom and is characterized neuropathologically by aExpand